Pro-longevity compounds extend Caenorhabditis elegans male lifespan and reproductive healthspan

Sex differences in aging are robust and ubiquitous. Demographic differences in aging generated by sex have long been recognized, but the underlying biological basis for these differences and the potential for sex-specific interventions remain understudied. To explore sex differences in the response to pro-longevity interventions, we utilized the C. elegans aging model and asked whether male lifespan and reproductive healthspan can be extended via compounds known to have pro-longevity effects in hermaphrodites. We tested seven different compounds at two concentrations each and found that lifespan was extended under all tested conditions. However, reproductive healthspan measured by mating success in late life improved under only two tested conditions, sulforaphane and metformin. These results demonstrate that lifespan and healthspan can be decoupled in C. elegans males and offer a new framework for screening pro-longevity compounds and for studying sex differences in aging in a classical aging model.

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Publication Details

Journal
GeroScience
Published
2026-02-17
DOI
https://doi.org/10.1007/s11357-026-02144-8
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Pro-longevity compounds extend Caenorhabditis elegans male lifespan and reproductive healthspan

Rose S. Al-Saadi, Patrick C. Phillips
GeroScience
Genetics, Aging, and Longevity in Model Organisms
article

Pro-longevity compounds extend Caenorhabditis elegans male lifespan and reproductive healthspan

Rose S. Al-Saadi, Patrick C. Phillips
article en

Abstract

Sex differences in aging are robust and ubiquitous. Demographic differences in aging generated by sex have long been recognized, but the underlying biological basis for these differences and the potential for sex-specific interventions remain understudied. To explore sex differences in the response to pro-longevity interventions, we utilized the C. elegans aging model and asked whether male lifespan and reproductive healthspan can be extended via compounds known to have pro-longevity effects in hermaphrodites. We tested seven different compounds at two concentrations each and found that lifespan was extended under all tested conditions. However, reproductive healthspan measured by mating success in late life improved under only two tested conditions, sulforaphane and metformin. These results demonstrate that lifespan and healthspan can be decoupled in C. elegans males and offer a new framework for screening pro-longevity compounds and for studying sex differences in aging in a classical aging model.

GeroScience
University of Oregon (US)
University of Oregon, National Institutes of Health, National Institute on Aging
Openalex Percentile: Top 52%
Genetics, Aging, and Longevity in Model Organisms
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